ID

42592

Descripción

BIBF1120 in Patients With Advanced FGFR3 Mutated,Overexpressed,or Wild Type Urothelial Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02278978

Link

https://clinicaltrials.gov/show/NCT02278978

Palabras clave

Versiones (1)
  1. 15.09.21 15.09.21 -
Titular de derechos de autor

National Taiwan University Hospital

Subido en

15. September 2021

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY-NC 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Urothelial Carcinoma NCT02278978

Inglés

Eligibility Urothelial Carcinoma NCT02278978

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
kps 60%
Descripción

Karnofsky Performance Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0206065
histological confirmation of urothelial carcinoma , with metastatic disease
Descripción

Urothelial carcinoma | Neoplasm metastasis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1519840
UMLS CUI [2]
C0027627
measurable disease
Descripción

Measurable disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1513041
previously treated with platinum-based chemotherapy administered
Descripción

Prior therapy with platinum-based chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C1514162
UMLS CUI [1,3]
C1514463
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
radiographic evidence of cavitary or necrotic tumours
Descripción

Radiographic evidence of cavitary tumors | Radiographic evidence of necrotic tumours

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C1510420
UMLS CUI [1,3]
C0034571
UMLS CUI [2,1]
C1300818
UMLS CUI [2,2]
C0034571
active brain metastasis.leptomeningeal metastasis
Descripción

Active brain metastasis | Leptomeningeal metastasis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0220650
UMLS CUI [1,2]
C0205177
UMLS CUI [2]
C1704231
chemotherapy, radiotherapy, targeted therapy with monoclonal antibodies or small tyrosine kinase inhibitors
Descripción

Chemotherapy | Radiotherapy | Targeted therapy with monoclonal antibodies | Targeted therapy with small tyrosine kinase inhibitors

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392920
UMLS CUI [2]
C1522449
UMLS CUI [3,1]
C2985566
UMLS CUI [3,2]
C0003250
UMLS CUI [4,1]
C2985566
UMLS CUI [4,2]
C1268567
grade 1 treatment-related toxicity from previous chemotherapy, radiotherapy, or targeted therapy
Descripción

Grade 1 treatment-related toxicity from previous chemotherapy, radiotherapy, or targeted therapy

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0877248
UMLS CUI [1,3]
C2826262
UMLS CUI [2,1]
C1522449
UMLS CUI [2,2]
C0877248
UMLS CUI [2,3]
C2826262
UMLS CUI [3,1]
C2985566
UMLS CUI [3,2]
C0877248
UMLS CUI [3,3]
C2826262
prior treatment with bibf 1120 or other vegfr inhibitors
Descripción

Prior therapy with nintedanib | Prior therapy with other VEGFR inhibitor

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2930789
UMLS CUI [1,2]
C1514463
UMLS CUI [2,1]
C2985521
UMLS CUI [2,2]
C1514463
UMLS CUI [2,3]
C2930789
UMLS CUI [2,4]
C1705847
significant cardiovascular diseases:
Descripción

Significant cardiovascular diseases

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0750502
pericardial effusion
Descripción

Pericardial effusion

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0031039
significant bleeding or thrombosis
Descripción

Significant bleeding | Significant thrombosis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019080
UMLS CUI [1,2]
C0750502
UMLS CUI [2,1]
C0040053
UMLS CUI [2,2]
C0750502
gastrointestinal disorders or abnormalities that would interfere with absorption of the study drug
Descripción

gGstrointestinal disorders or abnormalities that would interfere with absorption of the experimental drug

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0017178
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0304229
UMLS CUI [1,4]
C0237442
UMLS CUI [2,1]
C4023588
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0304229
UMLS CUI [2,4]
C0237442
major injuries within the past 10 days with incomplete wound healing and/or planned surgery during the on-treatment study period
Descripción

Recent major injuries that would interfere with wound healing | Surgery planned during the study period

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332677
UMLS CUI [1,2]
C0151692
UMLS CUI [1,3]
C0332185
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C1301732
UMLS CUI [2,3]
C0347984
UMLS CUI [2,4]
C0008976
Volver a la parte superior de la página

Similar models

Eligibility Urothelial Carcinoma NCT02278978

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Karnofsky Performance Status
Item
kps 60%
boolean
C0206065 (UMLS CUI [1])
Urothelial carcinoma | Neoplasm metastasis
Item
histological confirmation of urothelial carcinoma , with metastatic disease
boolean
C1519840 (UMLS CUI [1])
C0027627 (UMLS CUI [2])
Measurable disease
Item
measurable disease
boolean
C1513041 (UMLS CUI [1])
Prior therapy with platinum-based chemotherapy
Item
previously treated with platinum-based chemotherapy administered
boolean
C0392920 (UMLS CUI [1,1])
C1514162 (UMLS CUI [1,2])
C1514463 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Radiographic evidence of cavitary tumors | Radiographic evidence of necrotic tumours
Item
radiographic evidence of cavitary or necrotic tumours
boolean
C0027651 (UMLS CUI [1,1])
C1510420 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,3])
C1300818 (UMLS CUI [2,1])
C0034571 (UMLS CUI [2,2])
Active brain metastasis | Leptomeningeal metastasis
Item
active brain metastasis.leptomeningeal metastasis
boolean
C0220650 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
C1704231 (UMLS CUI [2])
Chemotherapy | Radiotherapy | Targeted therapy with monoclonal antibodies | Targeted therapy with small tyrosine kinase inhibitors
Item
chemotherapy, radiotherapy, targeted therapy with monoclonal antibodies or small tyrosine kinase inhibitors
boolean
C0392920 (UMLS CUI [1])
C1522449 (UMLS CUI [2])
C2985566 (UMLS CUI [3,1])
C0003250 (UMLS CUI [3,2])
C2985566 (UMLS CUI [4,1])
C1268567 (UMLS CUI [4,2])
Grade 1 treatment-related toxicity from previous chemotherapy, radiotherapy, or targeted therapy
Item
grade 1 treatment-related toxicity from previous chemotherapy, radiotherapy, or targeted therapy
boolean
C0392920 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
C2826262 (UMLS CUI [1,3])
C1522449 (UMLS CUI [2,1])
C0877248 (UMLS CUI [2,2])
C2826262 (UMLS CUI [2,3])
C2985566 (UMLS CUI [3,1])
C0877248 (UMLS CUI [3,2])
C2826262 (UMLS CUI [3,3])
Prior therapy with nintedanib | Prior therapy with other VEGFR inhibitor
Item
prior treatment with bibf 1120 or other vegfr inhibitors
boolean
C2930789 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C2985521 (UMLS CUI [2,1])
C1514463 (UMLS CUI [2,2])
C2930789 (UMLS CUI [2,3])
C1705847 (UMLS CUI [2,4])
Significant cardiovascular diseases
Item
significant cardiovascular diseases:
boolean
C0007222 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Pericardial effusion
Item
pericardial effusion
boolean
C0031039 (UMLS CUI [1])
Significant bleeding | Significant thrombosis
Item
significant bleeding or thrombosis
boolean
C0019080 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0040053 (UMLS CUI [2,1])
C0750502 (UMLS CUI [2,2])
gGstrointestinal disorders or abnormalities that would interfere with absorption of the experimental drug
Item
gastrointestinal disorders or abnormalities that would interfere with absorption of the study drug
boolean
C0017178 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C0237442 (UMLS CUI [1,4])
C4023588 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0304229 (UMLS CUI [2,3])
C0237442 (UMLS CUI [2,4])
Recent major injuries that would interfere with wound healing | Surgery planned during the study period
Item
major injuries within the past 10 days with incomplete wound healing and/or planned surgery during the on-treatment study period
boolean
C0332677 (UMLS CUI [1,1])
C0151692 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0543467 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0347984 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2,4])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial